A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104923



Internal ID20671963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97720808..97721047hg38UCSC Ensembl
chr3:97439652..97439891hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355618
Supporting Variants
Samples
Known GenesEPHA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00161


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